Medical Device Recalls
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1 result found
Recall Number: Z-0602-2026 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| BioFire Respiratory Panel 2.1, IVD, REF: 423742 (30 test kit) | 2 | 11/26/2025 |
FEI # 3002773840 BioFire Diagnostics, LLC |
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